Product Details

SNP ID

rs895869

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.2:148653363 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

GAGGAGAGGCTGATAGGAATAAGCC[A/C]TGAAGGAGACCAATGCAGATGGCAG

Phenotype

MIM: 611000

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

EPC2 PubMed Links

Additional Information

For this assay, SNP(s) [rs76761951] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

EPC2

Gene Name

enhancer of polycomb homolog 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015630.3		Intron			NP_056445.3
XM_011510941.2		Intron			XP_011509243.1
XM_011510943.2		Intron			XP_011509245.1

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